1413974-24-9

Upstream product

• 7647-01-0 hydrogenchloride 
• 1008-89-5 2-phenylpyridine 

Downstream Products

• 1447737-16-7 [Ir(2-phenylpyridine)₂(5-(p-methoxyphenyl)-4,5-dipyrrin)] 
• 1152172-07-0 [Ir(2-phenylpyridine)2-(4,7-diphenyl-1,10-phenanthroline)]Cl 
• 1449675-16-4 [Ir(phenylpyridine-H)2(3’-phosphino-2,2’:5’,2’’-terthiophene)-P,S]Cl 

Relevant academic research and scientific papers

Photophysical and electrochemical properties of phenanthroline-based bis-cyclometallated iridium complexes in aqueous and organic media

The electrochemical and photophysical properties of biscyclometallated iridium(III) complexes containing phenanthroline-based ligands have been investigated and compared in organic and aqueous media. Complexes having general formula [Ir(ppy)2(N

Development of Strong Visible-Light-Absorbing Cyclometalated Iridium(III) Complexes for Robust and Efficient Light-Driven Hydrogen Production

Weak light absorption of common Ir(III) complexes (e. g., using phenylpyridine as the ligand) has hindered their applications in photocatalytic hydrogen generation from water as an efficient photosensitizer. To address this issue, a series of cyclometalated Ir(III) complexes (Ir1–Ir5), featuring different electron-donating substituents to enhance the absorptivity, have been synthesized and studied as photosensitizers (PSs) for light-driven hydrogen production from water. Ir6–Ir7 were prepared as fundamental systems for comparisons. Electron donors, including 9-phenylcarbazole, triphenylamine, 4,4′-dimethoxytriphenylamine, 4,4′-di(N-hexylcarbazole)triphenylamine moieties were introduced on 6-(thiophen-2-yl)phenanthridine-based cyclometalating (C^N) ligands to explore the donor effect on the hydrogen evolution performance of these cationic Ir(III) complexes. Remarkably, Ir4 with 4,4′-dimethoxytriphenylamine achieved the highest turn-over number (TON) of 12 300 and initial turnover frequency (TOFi) of 394 h?1, with initial activity (activityi) of 547 000 μmol g?1 h?1 and initial apparent quantum yield (AQYi) of 9.59 %, under the illumination of blue light-emitting diodes (LEDs) for 105 hours, which demonstrated a stable three-component photocatalytic system with high efficiency. The TON (based on n(H2)/n(PSr)) in this study is the highest value reported to date among the similar photocatalytic systems using Ir(III) complexes with Pt nanoparticles as catalyst. The great potential of using triphenylamine-based Ir(III) PSs in boosting photocatalytic performance has also been shown.

A kinetic resolution strategy for the synthesis of chiral octahedral NHC-iridium(iii) catalysts

The transmetalation reaction of a chiral-bidentate NHC-silver complex to racemic [Ir(μ-Cl)(ppy)2]2 operates with kinetic resolution leading to chiral octahedral NHC-iridium(iii) complexes and enantio-enriched bis-cyclometalated iridium(iii) complexes. The iridium(iii) complexes demonstrated efficient catalytic activities in intermolecular [2+2] photocycloaddition reactions and in asymmetric Friedel-Crafts alkylations, respectively.

Compound and organic electroluminescent device

The invention discloses a compound and application of the compound to preparation of an organic electroluminescent device. The invention also provides the organic electroluminescent device, which comprises the compound. The compound provided by the invention is high in thermal stability, simple in synthesis process, low in the cost for a material purification process, and capable of improving thephotoelectric performance of the organic electroluminescent device.

Molecular tectonics: Heterometallic (Ir,Cu) grid-type coordination networks based on cyclometallated Ir(III) chiral metallatectons

A chiral-at-metal Ir(iii) organometallic metallatecton was synthesised as a racemic mixture and as enantiopure complexes and combined with Cu(ii) to afford a heterobimetallic (Ir,Cu) grid-type 2D coordination network.

Cyclometalated Ir(iii) complexes as targeted theranostic anticancer therapeutics: Combining HDAC inhibition with photodynamic therapy

The successful design and anticancer mechanistic studies of a series of cyclometalated Ir(iii) complexes with histone deacetylase inhibitory and photodynamic therapy (PDT) activities are reported. This journal is the Partner Organisations 2014.

BINUCLEAR METAL COMPLEX, AND ORGANIC ELECTROLUMINESCENCE ELEMENT USING SAME

The present invention relates to a novel binuclear metal complex, which has, for example, a biimidazole as a bridging ligand and is useful in particular as a material for an organic electroluminescence element.

An experimental and theoretical approach to the photophysical properties of some Rh and Ir complexes incorporating the dipyrromethene ligand

Rh and Ir complexes that contain meso-(p-methoxyphenyl)dipyrromethene (dipy) and phenylpyridine (ppy) ligands {i.e., [Rh(dipy)3], [Rh(ppy)2(dipy)] and [Ir(ppy)2(dipy)]} have been prepared and their electrochemical and luminescence behaviour are discussed and compared to results of theoretical calculations. The oxidation and reduction potentials, in agreement with the time-dependent (TD)-DFT calculations, indicate clearly that the HOMO-LUMO transitions are governed by the dipy ligand, which controls also the triplet excited-state emission. However, in luminescence, the two Rh complexes exhibit, in addition to a dipy-centred triplet emission, luminescence from the singlet excited state, which predominates at room temperature, due to a less important influence of the heavy-metal effect in Rh than in Ir complexes. Although the TD-DFT results are in very good agreement with the experimental emission spectra from the dipy-centred triplet excited state, this is not the case for the absorption spectra of the complexes and free dipy ligand. Copyright

Luminescent, enantiopure, phenylatopyridine iridium-based coordination capsules

The first molecular capsule based on an [Ir(ppy)2]+ unit (ppy = 2-phenylatopyridine) has been prepared. Following the development of a method to resolve rac-[(Ir(ppy)2Cl)2] into its enantiopure forms, homochiral Ir6L4 octahedra where obtained with the tritopic 1,3,5-tricyanobenzene. Solution studies and X-ray diffraction show that these capsules encapsulate four of the six associated counteranions and that these can be exchanged for other anionic guests. Initial photophysical studies have shown that an ensemble of weakly coordinating ligands can lead to luminescence not present in comparable mononuclear systems.